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clinical_trial_csr_template

Informed consent was obtained from all participants before any study-specific procedures. The informed consent process included: - Written information about study purpose, procedures, risks, and benefits - Opportunity to ask questions -…

  • Skills
  • Scientific
  • 0

What it does and how to use it

A skill that teaches Claude Code to do scientific tasks well. It is packaged knowledge the model uses whenever it is relevant.

  1. Install the skill (command above).
  2. In Claude Code, describe what you need - the skill turns on by itself when the context fits.
  3. No commands to memorize: you talk in plain language and the skill does the rest.

Install (Claude Code)

mkdir -p .claude/skills/clinical-trial-csr-template && curl -fsSL https://doutorai.pt/data/lib/skills__clinical-trial-csr-template.md -o .claude/skills/clinical-trial-csr-template/SKILL.md

Paste this command into the terminal, in your project folder, and the component installs automatically.

Content

# Clinical Study Report (CSR) Template
## ICH-E3 Format

---

# TITLE PAGE

**Study Title:** [Full descriptive title including compound, indication, phase]

**Protocol Number:** [Sponsor protocol number]  
**Protocol Version:** [Final protocol version and date]

**Sponsor:** [Company name and address]  
**Compound/Drug Name:** [Generic and proprietary names, compound code]  
**Indication:** [Therapeutic area and specific indication studied]

**Study Phase:** [I / II / III / IV]  
**Study Type:** [Interventional / Observational]

**Report Date:** [MM/DD/YYYY]  
**Report Version:** [Version numb

- 🔒 Full content on the Pro plan (€7.99/month) -

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